Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
Guran, Tulay, Buonocore, Federica, Saka, Nurcin, Ozbek, Mehmet Nuri, Aycan, Zehra, Bereket, Abdullah, Bas, Firdevs, Darcan, Sukran, Bideci, Aysun, Guven, Ayla, Demir, Korcan, Akinci, Aysehan, Buyukinan, Muammer, Aydin, Banu Kucukemre, Turan, Serap, Agladioglu, Sebahat Yilmaz, Atay, Zeynep, Abali, Zehra Yavas, Tarim, Omer, Catli, Gonul, Yuksel, Bilgin, Akcay, Teoman, Yildiz, Metin, Ozen, Samim, Doger, Esra, Demirbilek, Huseyin, Ucar, Ahmet, Isik, Emregul, Ozhan, Bayram, Bolu, Semih, Ozgen, Ilker Tolga, Suntharalingham, Jenifer P, Achermann, John C
Published in The journal of clinical endocrinology and metabolism (01.01.2016)
Published in The journal of clinical endocrinology and metabolism (01.01.2016)
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Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets
Guven, Ayla, Al‐Rijjal, Roua A., BinEssa, Huda A., Dogan, Durmuş, Kor, Yılmaz, Zou, Minjing, Kaya, Namik, Alenezi, Anwar F., Hancili, Suna, Tarım, Ömer, Baitei, Essa Y., Kattan, Walaa E, Meyer, Brian F., Shi, Yufei
Published in Clinical endocrinology (Oxford) (01.07.2017)
Published in Clinical endocrinology (Oxford) (01.07.2017)
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Clinical and Laboratory Follow up of Pediatric Craniopharyngioma Cases
Söbü, Elif, Eren, Erdal, Sevinir, Betül, Taşkapılıoğlu, M. Özgür, Tarım, Ömer
Published in Güncel pediatri (01.12.2020)
Published in Güncel pediatri (01.12.2020)
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Pediatric patients with pheochromocytoma: Experience of a tertiary health center
Eren, Erdal, Saglam, Halil, Caliskan, Yusuf, Kiristioglu, Irfan, Tarim, Omer
Published in Pediatrics international (01.10.2015)
Published in Pediatrics international (01.10.2015)
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Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community
Cangul, Hakan, Aycan, Zehra, Olivera-Nappa, Alvaro, Saglam, Halil, Schoenmakers, Nadia A., Boelaert, Kristien, Cetinkaya, Semra, Tarim, Omer, Bober, Ece, Darendeliler, Feyza, Bas, Veysel, Demir, Korcan, Aydin, Banu K., Kendall, Michaela, Cole, Trevor, Högler, Wolfgang, Chatterjee, V. Krishna K., Barrett, Timothy G., Maher, Eamonn R.
Published in Clinical endocrinology (Oxford) (01.08.2013)
Published in Clinical endocrinology (Oxford) (01.08.2013)
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Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
Cangul, Hakan, Liao, Xiao-Hui, Schoenmakers, Erik, Kero, Jukka, Barone, Sharon, Srichomkwun, Panudda, Iwayama, Hideyuki, Serra, Eva G, Saglam, Halil, Eren, Erdal, Tarim, Omer, Nicholas, Adeline K, Zvetkova, Ilona, Anderson, Carl A, Frankl, Fiona E Karet, Boelaert, Kristien, Ojaniemi, Marja, Jääskeläinen, Jarmo, Patyra, Konrad, Löf, Christoffer, Williams, E Dillwyn, Soleimani, Manoocher, Barrett, Timothy, Maher, Eamonn R, Chatterjee, V Krishna, Refetoff, Samuel, Schoenmakers, Nadia
Published in JCI insight (18.10.2018)
Published in JCI insight (18.10.2018)
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Retrospective Evaluation of Patients Diagnosed with Osteogenesis Imperfecta
Aslan, Mustafa Törehan, Eren, Erdal, Sağlam, Halil, Tarım, Ömer
Published in Güncel pediatri (01.04.2017)
Published in Güncel pediatri (01.04.2017)
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Neonatal adrenal insufficiency: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report
Yiğit, Şule, Türkmen, Münevver, Tuncer, Oğuz, Taşkın, Erdal, Güran, Tülay, Abacı, Ayhan, Çatlı, Gönül, Tarım, Ömer
Published in Turk Pediatri Arsivi (01.01.2018)
Published in Turk Pediatri Arsivi (01.01.2018)
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Clinical course of hyperprolactinemia in children and adolescents: a review of 21 cases
Eren, Erdal, Yapıcı, Şenay, Çakır, Esra Deniz Papatya, Ceylan, Latife Aytekin, Sağlam, Halil, Tarım, Ömer
Published in Journal of clinical research in pediatric endocrinology (01.06.2011)
Published in Journal of clinical research in pediatric endocrinology (01.06.2011)
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TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis
Cangul, Hakan, Aycan, Zehra, Saglam, Halil, Forman, Julia R., Cetinkaya, Semra, Tarim, Omer, Bober, Ece, Cesur, Yasar, Kurtoglu, Selim, Darendeliler, Feyza, Bas, Veysel, Eren, Erdal, Demir, Korcan, Kiraz, Aslihan, Aydin, Banu K., Karthikeyan, Ambika, Kendall, Michaela, Boelaert, Kristien, Shaw, Nick J., Kirk, Jeremy, Högler, Wolfgang, Barrett, Timothy G., Maher, Eamonn R.
Published in Journal of Pediatric Endocrinology and Metabolism (2012)
Published in Journal of Pediatric Endocrinology and Metabolism (2012)
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A rare cause of precocious puberty: hepatoblastoma
Eren, Erdal, Demirkaya, Metin, Çakır, Esra D Papatya, Sevinir, Betül, Sağlam, Halil, Tarım, Ömer
Published in Journal of clinical research in pediatric endocrinology (01.12.2009)
Published in Journal of clinical research in pediatric endocrinology (01.12.2009)
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